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US3882145A - Halogenated N-substituted thiocarboxy maleimides - Google Patents

Halogenated N-substituted thiocarboxy maleimides Download PDF

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US3882145A
US3882145A US317571A US31757172A US3882145A US 3882145 A US3882145 A US 3882145A US 317571 A US317571 A US 317571A US 31757172 A US31757172 A US 31757172A US 3882145 A US3882145 A US 3882145A
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maleimide
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maleimides
halogenated
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William E Bissinger
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Wyeth Holdings LLC
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PPG Industries Inc
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    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D207/00—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/44—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members
    • C07D207/444—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5
    • C07D207/448—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5 with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. maleimide
    • C07D207/452—Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having three double bonds between ring members or between ring members and non-ring members having two doubly-bound oxygen atoms directly attached in positions 2 and 5 with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. maleimide with hydrocarbon radicals, substituted by hetero atoms, directly attached to the ring nitrogen atom

Definitions

  • ABSTRACT Disclosed are 2,3-clihalo and Z-halo-N-substituted thiocarboxy maleimides of the formula I n-c-s-R x" 0
  • X is halogen
  • X is halogen or H
  • R is an organic radical containing up to about 12 carbon atoms.
  • the compounds of the present invention possess postemergent herbicidal activity and many of the compounds possess viricidal activity.
  • X is halogen, i.e., fluorine, chlorine, bromine, or iodine; X is halogen or H; and R is an organic radical containing from 1 to about 12 carbon atoms. Typically R will contain from 1 to carbon atoms and preferably will contain from 1 to 6 carbon atoms.
  • R may be straight or branched chain aliphatic such as straight or branched chain alkane, straight or branched chain alkene or straight or branched chain haloalkane or haloalkene.
  • the R moi ety may also be cycloaliphatic such as cycloalkane, cycloalkene, cyclohaloalkane, or cyclohaloalkene.
  • R may be an aromatic moiety of from 6 to about 12 carbon atoms; for example R may be phenyl, alkylsubstituted phenyl, alkoxy-substituted phenyl, or halogen-substituted phenyl.
  • X and X are chlorine and R is an aliphatic group containing from 1 to about 6 carbon atoms.
  • R groups of the preferred embodiment are methyl, 2- chloro-ethyl, isopropyl, 2,3-dibromo butyl, isopentyl, and 2-chloro-3-hexenyl.
  • the halogenated maleimides necessary for preparation of the desired compound can be prepared by known methods.
  • 2'fluoromaleimide can be prepared by the reaction of 2-chloromaleimide with potassium fluoride in dimethyl formamide (see J. Am. Chem. Soc, 78, 6034 (1956) and 81, 2674 (1959)).
  • the difluoro compound, 2,3-difluoromaleimide may be prepared by the reaction of 2,3-dichloromaleimide with potassium fluoride in dimethyl fonnamide.
  • the monochloro compound, 2-chloromaleimide is obtained along with 2,3-dich1oromaleimide by the chlorination of succinimide (G. L. Ciamician and P.
  • the monobromo compound, Z-bromomaleimide may be prepared by the bromination of succinirnide as reported by K. Loscher and R. Kusserow in Chem. Ber. 21, 2718 (1888).
  • the dibromo compound, 2,3-dibromomaleimide is also prepared by the reaction of bromine with succinimide as reported by G. L. Ciaimician and P. Silber in Chem. Ber. 17, 553 (1884). It is reported by A. P. Terentjew and W. W. Tschelinzew in Chem. Ber. 58B, 66 (1925) that 2,3- diiodomaleimide is prepared by the nitric acid oxidation of diiodo-a-acetylpyrrole.
  • the reaction between the halogenated maleimide and chlorothioformate may be carried out in a liquid medium provided by an organic solvent which is inert to the reactants and products and in which is dissolved an acid acceptor.
  • organic solvents include benzene, ethyl ether, dioxane, toluene, xylene, carbon tetrachloride, and chloroform.
  • Acid acceptors which may be employed include triethylamine, pyridine, and N,N-
  • the reaction temperature may range from the freez ing point to the boiling point of the system. In general, a reaction temperature of from 20 to 100C. is desirable, with a temperature of from 0 to C. being preferred.
  • the reaction was carried out in a 1,000-milliliter, 3- necked, round-bottomed flask equipped with two C1 cylinders in parallel attached to a gas inlet tube with one cylinder operating at a time.
  • a thermometer H 80. bubbler (for judging gas flow), a glass wool filled dropout trap, an HCl scrubber through which water was slowly dropped, and an Erlenmeyer collection flask under the scrubber whose contents were periodically titrated for l-lCl by-product.
  • the reaction flask contents were stirred by a motor-driven Teflon paddle and heated by two 275-watt sunlamps which provided catalytic radiation.
  • the reaction flask was charged with 300 grams (3.03 moles) of succinimide after having been purged with purified nitrogen the preceding day.
  • the flask was heated to 128C. with a heating mantle to melt the succinimide which had a melting point of 125C. Subsequent heating was accomplished solely by the sunlamps.
  • 135C chlorine addition to the light tan melt was started with the melt changing to a honey" yellow color shortly thereafter.
  • the average chlorine addition rate during the 22.5-hour run was 53 grams per hour.
  • the temperature was maintained at 140C. during the first 16 hours and at 165C. thereafter. After 22.5 hours the temperature suddenly decreased to 150C. for no apparent reason, with the reaction mixture color becoming a deep red.
  • Part B A portion of the crude product from the bottom portion of the reactor flask was sublimed in a 1,000-milliliter Erlenmeyer flask, yielding 47 grams of a light yellow product. This material was recrystallized from 30 milliliters of absolute ethanol, yielding 27.2 grams of light yellow crystals having a melting point of 173 to 176C. These crystals were next recrystallized from 39 grams of 95 per cent ethanol, yielding 22.5 grams (22.5/47 47.8 percent recovery) of white crystals having a melting point of 178 to 180C.
  • Part D Another portion of the crude reaction product from the bottom of the reactor was sublimed yielding 87 grams of a slightly olf-white product. This material was recrystallized in 48 milliliters of hot absolute ethanol, yielding 53.5 grams of white crystals having a melting point of from 174 to 177C. These crystals were recrystallized from 46 grams of hot 95 per cent ethanol, yielding 42.8 grams (42.8/87 49.2 percent recovery) of white crystals having a melting point of from 178 to 180C.
  • EXAMPLE 11 A reactor was set up which consisted of a 100- milliliter, 3-necked flask equipped with a magnetic stirrer, thermometer, and two dropping funnels. A solution of 2,3-dichloromaleimide (3.3 grams, .02 mole) in 25 milliliters of benzene was added to the flask. From the dropping funnels 2.8 grams (0.02 mole) of isopropylthiolchloroformate, prepared by the method described in Example IV of US. Pat. No.
  • feetive viricides are especially effective against the tobacco mosaic virus.
  • formulations containing from about 0.05 to about 90 per cent by weight of the maleimide are applied to the plants being treated.
  • Typical formulations contain from about 25 to about 75 per cent and formulations containing from about 25 to 50 per cent are preferred.
  • the type of formulation may vary. Solutions and suspensions of the maleimide are effective. The usual method of applying solutions or suspensions of the compound being used is to drench the area of application. Sprays, showers, mists, and dips may be used for this purpose.
  • Typical solvents which may be employed to prepare maleimide formulations for application include naphtha, toluene, xylene, and isopheron.
  • the maleimide being employed is dissolved in the carrier at a level of 2 to 6 and typically 3 to 4 pounds per gallon. Suspending agents are employed when needed. This solution is then combined with about 50 gallons of water to form an emulsion of the dissolved maleimide in water which is applied to the plants being treated by the methods set out above.
  • the maleimide may also be applied to the area to be treated in the form of granules.
  • Granular formulations are prepared by dissolving the maleimide in a high boiling petroleum solvent such as l-lans Solvent (a heavy aromatic naphtha) or a xylene and spraying the resulting solution through a nozzle manifold mounted in a tumbler blender onto presized granules typically composed of attapulgite or bentonite.
  • concentration of toxicant will normally range from 1 per cent to 30 per cent, typically from 5 to 20 per cent, by weight of the formulation with the solvent accounting for from 2 per cent to 20 per cent, and typically from 5 to per cent, by weight of the formulation.
  • the granules, whose particle size will normally be /30 and preferably 24/48 on the US Standard Sieve Series, are applied directly to the area to be treated such as by use of a broadcast spreader.
  • compositions of the instant invention are in the form of a wettable powder.
  • the powders are prepared by mixing the maleimide with a diluent such as a clay, e.g., talc, kalonite, or a pyrophylite, or a synthetic silica such as l-li-Sil 233 marketed by PPG lndustries, lnc.
  • a diluent such as a clay, e.g., talc, kalonite, or a pyrophylite
  • a synthetic silica such as l-li-Sil 233 marketed by PPG lndustries, lnc.
  • the toxicant will account for 25 to 80 per cent by weight and typically 50 to 75 per cent of the formulation.
  • the resulting mixture is ground, typically in a hammer mill, to yield a product of which 99 per cent or more has a particle size of 200 mesh.
  • the particulate formulation is normally combined with up to 5 weight per cent of each of a dispersing agent such as Polyfon F (a sodium lignosulfonate marketed by West Vaco) and a wetting agent such as lgepon T-77 (sodium-N-methyl-N-oleoyltaurate marketed by GAF).
  • a dispersing agent such as Polyfon F (a sodium lignosulfonate marketed by West Vaco) and a wetting agent such as lgepon T-77 (sodium-N-methyl-N-oleoyltaurate marketed by GAF).
  • lgepon T-77 sodium-N-methyl-N-oleoyltaurate marketed by GAF
  • the formulation is applied so as to provide 1 to 100 pounds of the maleimide per acre with an application level of l to 15 pounds per acre being typical and a level of 2 to 12 pounds per acre being preferred.
  • EXAMPLE lll Appropriate weed species were seeded by growthtime requirement schedules in individual, disposable, 3-inch square containers containing about 2 inches of soil and maintained under greenhouse conditions. When all the weeds had reached suitable growth development (generally first-true leaf stage) plants appropriate to pertaining test requirements were selected for uniformity of growth and development. One container of each weed, averaging up to plants per individual container, was then placed on a carrying tray for treatment.
  • the compound being tested i.e., 2,3-dich1oro-N- isopropyl-thiocarboxy maleimide, was formulated in a solvent mixture of percent acetone, 8 percent methanol, and 2 percent dimethylformamide by volume.
  • the carrying trays of containers were placed on a conveyer belt having a linear speed of 1.5 miles per hour. Each tray, as it was carried by the conveyer belt, tripped a microswitch which, in turn, activated a solenoid valve and released the formulated composition in a spray equivalent to 10 pounds of 2,3-dichloro-N-isopropylthiocarboxy maleimide per acre.
  • the containers were then removed to the greenhouse and held for observation. The treated plants were observed daily for interim response with final observations being made about 14 days after treatment.
  • the maleimide being tested was dissolved in a solvent composition comprised of 4 milliliters sorbitan trioleate (Span 85), l milliliter of a polyoxyalkylene derivative of sorbitan monooleate (Tween 80), and 1995 mi]- liliters of acetone.
  • a solvent composition comprised of 4 milliliters sorbitan trioleate (Span 85), l milliliter of a polyoxyalkylene derivative of sorbitan monooleate (Tween 80), and 1995 mi]- liliters of acetone.
  • the solution was applied to the test plants with a spraying device having a pressurized valve control at 40 pounds pressure for 60 seconds, thereby assuring complete coverage of the plant surface.
  • the treated plants had air dried, they were inoculated by spraying with extract from tobacco mosaic virus infected leaves and carborundum.
  • the carborundum which was kept in suspension by constant agitation of the solution, caused the surface tissue of the plant to rupture
  • a halogenated N-substituted thiocarboxy maleimide represented by the formula:
  • X is halogen; X is halogen or H; and R is alkyl, alkenyl, cycloalkyl, cycloalkenyl, haloalkyl, haloalkenyl, phenyl, alkyl phenyl, alkoxyphenyl or halophenyl containing 12 carbon atoms or less, which comprises reacting a halogenated maleimide of the formula:

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  • Indole Compounds (AREA)

Abstract

In the above formula, X is halogen; X'' is halogen or H; and R is an organic radical containing up to about 12 carbon atoms. The compounds of the present invention possess postemergent herbicidal activity and many of the compounds possess viricidal activity.

Disclosed are 2,3-dihalo and 2-halo-N-substituted thiocarboxy maleimides of the formula

Description

United States Patent [1 1 Bissinger May 6,1975
[ HALOGENATED N-SUBSTITUTED Tl-IIOCARBOXY MALEIMIDES [52] US. Cl. 260/326.4; 71/95; 424/274 [51] Int. Cl C07d 27/18 [58] .Field of Search 260/3264 References Cited UNITED STATES PATENTS 3,340,263 9/l967 Staehelin et al. 260/3265 X Primary Examiner-1oseph A. Narcavage Attorney, Agent, or Firm-Mark Levin [57] ABSTRACT Disclosed are 2,3-clihalo and Z-halo-N-substituted thiocarboxy maleimides of the formula I n-c-s-R x" 0 In the above formula, X is halogen; X is halogen or H; and R is an organic radical containing up to about 12 carbon atoms. The compounds of the present invention possess postemergent herbicidal activity and many of the compounds possess viricidal activity.
5 Claims, No Drawings HALOGENATED N-SUBSTITUTED THIOCARBOXY MALEIMIDES The present invention relates to halogenated N- substituted thiocarboxy maleimides of the formula:
wherein X is halogen, i.e., fluorine, chlorine, bromine, or iodine; X is halogen or H; and R is an organic radical containing from 1 to about 12 carbon atoms. Typically R will contain from 1 to carbon atoms and preferably will contain from 1 to 6 carbon atoms.
in the above formula, R may be straight or branched chain aliphatic such as straight or branched chain alkane, straight or branched chain alkene or straight or branched chain haloalkane or haloalkene. The R moi ety may also be cycloaliphatic such as cycloalkane, cycloalkene, cyclohaloalkane, or cyclohaloalkene. in addition, R may be an aromatic moiety of from 6 to about 12 carbon atoms; for example R may be phenyl, alkylsubstituted phenyl, alkoxy-substituted phenyl, or halogen-substituted phenyl.
In a preferred embodiment of the present invention, X and X are chlorine and R is an aliphatic group containing from 1 to about 6 carbon atoms. Examples of R groups of the preferred embodiment are methyl, 2- chloro-ethyl, isopropyl, 2,3-dibromo butyl, isopentyl, and 2-chloro-3-hexenyl.
Compounds within the scope of the present invention are:
2,3-diiodo-N-isobutylthiocarboxy maleimide 2,3-diiodo-N-heptenylthiocarboxy maleimide 2-iodo-N-nonylthiocarboxy maleimide 2,3-dichloro-N-isopropylthiocarboxy maleimide 2,3-dichloro-N-allylthiocarboxy maleimide 2,3-dichloro-N-2,3-dibromopropylthiocarboxy maleimide 2,3-dichloro-N-3-methoxyphenylthiocarboxy maleimide 2,3-dichloro-N-Z-chloroallylthiocarboxy maleimide 2,3-dich1oro-N-cyclopentylthiocarboxy maleimide 2-chloro-N-isopropylthiocarboxy maleimide 2-chloro-N-dodecylthiocarboxy maleimide 2-chloro-N-3,4-dichlorohexylthiocarboxy maleimide 2-chloro-N-2-chlorophenylthiocarboxy maleimide 2-chloro-N-cyclohexylthiocarboxy maleimide 2,3-dibromo-N-propylthiocarboxy maleimide 2,3-dibromo-N-2-hexenylthiocarboxy maleimide 2,3dibromoN-octylthiocarboxy maleimide 2-bromo-N-2,3-dichlorophenylthiocarboxy mide 2-bromo-N-isopropylthiocarboxy maleimide 2,3-dif1uoro-N-pentylthiocarboxy maleimide 2,3 dithaoro-N-allylthiocarboxy maleimide 2,3-difiuoro-N-2,3-dichlorophenylthiocarboxy maleimide lflmN-LN-Z-fluoroallflthiocmboxy maleimide malei- 2--fluoro-N-2,3,4trimethylphenylthiocarboxy malei- 2 -41 1 .us I' 0 C1-C-S-R where R is an organic radical having from 1 to about 12 carbon atoms.
The halogenated maleimides necessary for preparation of the desired compound can be prepared by known methods. For example, 2'fluoromaleimide can be prepared by the reaction of 2-chloromaleimide with potassium fluoride in dimethyl formamide (see J. Am. Chem. Soc, 78, 6034 (1956) and 81, 2674 (1959)). The difluoro compound, 2,3-difluoromaleimide, may be prepared by the reaction of 2,3-dichloromaleimide with potassium fluoride in dimethyl fonnamide. The monochloro compound, 2-chloromaleimide, is obtained along with 2,3-dich1oromaleimide by the chlorination of succinimide (G. L. Ciamician and P. Silber, Chem. Ber. 16, 2394 (1883)). It is also reported to be obtained by the reaction of chloromaleic anhydride with ammonia over alumina (British Pat. No. 1,1 16,125). The bromo-chloro compound, 2-bromo-3- chloromaleimide, may be prepared by the treatment of 2,3,5-trichloropyrrole with 1.5 moles of bromine in acetic acid or by the oxidation of 2,4,5-trichloro-3- bromopyrrole with nitric acid as reported in Beilstein, 21, 404 and by Mazzara and Borgo in Gazz. Chim. ltal. 34 I1, 125, 181 (1904). The monobromo compound, Z-bromomaleimide may be prepared by the bromination of succinirnide as reported by K. Loscher and R. Kusserow in Chem. Ber. 21, 2718 (1888). The dibromo compound, 2,3-dibromomaleimide, is also prepared by the reaction of bromine with succinimide as reported by G. L. Ciaimician and P. Silber in Chem. Ber. 17, 553 (1884). It is reported by A. P. Terentjew and W. W. Tschelinzew in Chem. Ber. 58B, 66 (1925) that 2,3- diiodomaleimide is prepared by the nitric acid oxidation of diiodo-a-acetylpyrrole.
The reaction between the halogenated maleimide and chlorothioformate may be carried out in a liquid medium provided by an organic solvent which is inert to the reactants and products and in which is dissolved an acid acceptor. Preferred solvents include benzene, ethyl ether, dioxane, toluene, xylene, carbon tetrachloride, and chloroform. Acid acceptors which may be employed include triethylamine, pyridine, and N,N-
dimethyl aniline.
The reaction temperature may range from the freez ing point to the boiling point of the system. In general, a reaction temperature of from 20 to 100C. is desirable, with a temperature of from 0 to C. being preferred.
The following examples illustrate how the present invention may be practiced.
EXAMPLE 1 2,3-dichl0romaleimide was prepared by the photochlorination of succinimide as represented by the following equation:
The reaction was carried out in a 1,000-milliliter, 3- necked, round-bottomed flask equipped with two C1 cylinders in parallel attached to a gas inlet tube with one cylinder operating at a time. On the exit side of the reaction flask was attached a thermometer, H 80. bubbler (for judging gas flow), a glass wool filled dropout trap, an HCl scrubber through which water was slowly dropped, and an Erlenmeyer collection flask under the scrubber whose contents were periodically titrated for l-lCl by-product. The reaction flask contents were stirred by a motor-driven Teflon paddle and heated by two 275-watt sunlamps which provided catalytic radiation.
The reaction flask was charged with 300 grams (3.03 moles) of succinimide after having been purged with purified nitrogen the preceding day. The flask was heated to 128C. with a heating mantle to melt the succinimide which had a melting point of 125C. Subsequent heating was accomplished solely by the sunlamps. At 135C. chlorine addition to the light tan melt was started with the melt changing to a honey" yellow color shortly thereafter. The average chlorine addition rate during the 22.5-hour run was 53 grams per hour. The temperature was maintained at 140C. during the first 16 hours and at 165C. thereafter. After 22.5 hours the temperature suddenly decreased to 150C. for no apparent reason, with the reaction mixture color becoming a deep red. Upon a continuing temperature decrease, the reaction was terminated after an additional minutes. Total weight of chlorine used during the reaction was 1202 grams by cylinder weight difference. Total weight of crude product, which contained some dissolved C1 gas, was 455.5 grams. The crude product was broken down into four fractions which were purified as follows:
Part A Seventy-five grams of crude product which had been deposited on the upper flask walls were recrystallized from 75 milliliters of hot absolute ethanol, yielding 47 grams of light yellow crystals having a melting point of from l75 to 178C. These crystals were then recrystallized from 53 grams of 95 per cent ethanol, yielding 36.4 grams (36.4/75 =48.5 percent recov cry) of white crystals having a melting point of from 178 to 180C.
Part B A portion of the crude product from the bottom portion of the reactor flask was sublimed in a 1,000-milliliter Erlenmeyer flask, yielding 47 grams of a light yellow product. This material was recrystallized from 30 milliliters of absolute ethanol, yielding 27.2 grams of light yellow crystals having a melting point of 173 to 176C. These crystals were next recrystallized from 39 grams of 95 per cent ethanol, yielding 22.5 grams (22.5/47 47.8 percent recovery) of white crystals having a melting point of 178 to 180C.
Part C Two hundred five grams of crude product from the reactor flask were recrystallized from 1 18 milliliters of absolute ethanol, yielding 1 18 grams of medium yellow crystals having a melting point of 174 to 177C. These crystals were then recrystallized from 81.5 grams of ethanol, yielding 70.3 grams (70.3/205 34.4 percent recovery) of light yellow crystals hav ing a melting point of from 178 to 180C.
Part D Another portion of the crude reaction product from the bottom of the reactor was sublimed yielding 87 grams of a slightly olf-white product. This material was recrystallized in 48 milliliters of hot absolute ethanol, yielding 53.5 grams of white crystals having a melting point of from 174 to 177C. These crystals were recrystallized from 46 grams of hot 95 per cent ethanol, yielding 42.8 grams (42.8/87 49.2 percent recovery) of white crystals having a melting point of from 178 to 180C.
Although the crystal color did not affect the melting points of the final purified fractions, Parts A, B, and D were combined while Part C was kept s vparate due to its yellow color. The reaction went to about per cent completion with the final purified product amounting to 33.6 per cent of the theoretical yield based upon succinimide.
EXAMPLE 11 A reactor was set up which consisted of a 100- milliliter, 3-necked flask equipped with a magnetic stirrer, thermometer, and two dropping funnels. A solution of 2,3-dichloromaleimide (3.3 grams, .02 mole) in 25 milliliters of benzene was added to the flask. From the dropping funnels 2.8 grams (0.02 mole) of isopropylthiolchloroformate, prepared by the method described in Example IV of US. Pat. No. 3,093,537, in 10 milliliters of benzene and 2.0 grams (0.02 mole) of triethylamine in 5 milliliters of benzene were added simultaneously over 15 minutes with the temperature being maintained at less than 25C. by an ice bath.
The reaction mixture was maintained at room temperature over night and suction filtered to remove amine hydrochloride. The filtrate was evaporated to dryness and the brown residue recrystallized from a mixture of ether and hexane. There resulted 3.9 grams (72.6 percent yield) of 2,3-dichloro-N-isopropylthiocarboxy maleimide:
l 1: c s ca {0 011 01 The product consisted of tan crystals having a melting point of 87 to C.
Elemental analysis of the product provided the following results:
Calculaled for C H N C H CI,NO;,S 35.82% 2.61% 5.22%
Found Run 1 35.95 2.68 5.07
Run 2 35.95 2.53 5.08 Average 35.95 2.61 5.08
feetive viricides and are especially effective against the tobacco mosaic virus.
1n application, formulations containing from about 0.05 to about 90 per cent by weight of the maleimide are applied to the plants being treated. Typical formulations contain from about 25 to about 75 per cent and formulations containing from about 25 to 50 per cent are preferred.
The type of formulation may vary. Solutions and suspensions of the maleimide are effective. The usual method of applying solutions or suspensions of the compound being used is to drench the area of application. Sprays, showers, mists, and dips may be used for this purpose.
Typical solvents which may be employed to prepare maleimide formulations for application include naphtha, toluene, xylene, and isopheron. In one method of application, the maleimide being employed is dissolved in the carrier at a level of 2 to 6 and typically 3 to 4 pounds per gallon. Suspending agents are employed when needed. This solution is then combined with about 50 gallons of water to form an emulsion of the dissolved maleimide in water which is applied to the plants being treated by the methods set out above.
The maleimide may also be applied to the area to be treated in the form of granules. Granular formulations are prepared by dissolving the maleimide in a high boiling petroleum solvent such as l-lans Solvent (a heavy aromatic naphtha) or a xylene and spraying the resulting solution through a nozzle manifold mounted in a tumbler blender onto presized granules typically composed of attapulgite or bentonite. The concentration of toxicant will normally range from 1 per cent to 30 per cent, typically from 5 to 20 per cent, by weight of the formulation with the solvent accounting for from 2 per cent to 20 per cent, and typically from 5 to per cent, by weight of the formulation. The granules, whose particle size will normally be /30 and preferably 24/48 on the US Standard Sieve Series, are applied directly to the area to be treated such as by use of a broadcast spreader.
An alternative manner of applying the compositions of the instant invention to the area to be treated is in the form of a wettable powder. The powders are prepared by mixing the maleimide with a diluent such as a clay, e.g., talc, kalonite, or a pyrophylite, or a synthetic silica such as l-li-Sil 233 marketed by PPG lndustries, lnc. Normally the toxicant will account for 25 to 80 per cent by weight and typically 50 to 75 per cent of the formulation. The resulting mixture is ground, typically in a hammer mill, to yield a product of which 99 per cent or more has a particle size of 200 mesh. The particulate formulation is normally combined with up to 5 weight per cent of each of a dispersing agent such as Polyfon F (a sodium lignosulfonate marketed by West Vaco) and a wetting agent such as lgepon T-77 (sodium-N-methyl-N-oleoyltaurate marketed by GAF). The resulting powder is applied to the area to be treated by dispersing it in water to provide a suspension ranging from 0.5 to 5 per cent by weight of toxicant. The suspension is then applied to the area to be treated such as by spraying.
In general, the formulation is applied so as to provide 1 to 100 pounds of the maleimide per acre with an application level of l to 15 pounds per acre being typical and a level of 2 to 12 pounds per acre being preferred.
EXAMPLE lll Appropriate weed species were seeded by growthtime requirement schedules in individual, disposable, 3-inch square containers containing about 2 inches of soil and maintained under greenhouse conditions. When all the weeds had reached suitable growth development (generally first-true leaf stage) plants appropriate to pertaining test requirements were selected for uniformity of growth and development. One container of each weed, averaging up to plants per individual container, was then placed on a carrying tray for treatment.
The compound being tested, i.e., 2,3-dich1oro-N- isopropyl-thiocarboxy maleimide, was formulated in a solvent mixture of percent acetone, 8 percent methanol, and 2 percent dimethylformamide by volume.
The carrying trays of containers were placed on a conveyer belt having a linear speed of 1.5 miles per hour. Each tray, as it was carried by the conveyer belt, tripped a microswitch which, in turn, activated a solenoid valve and released the formulated composition in a spray equivalent to 10 pounds of 2,3-dichloro-N-isopropylthiocarboxy maleimide per acre. The containers were then removed to the greenhouse and held for observation. The treated plants were observed daily for interim response with final observations being made about 14 days after treatment.
Each result is reported as an injury rating which is represented as follows: 0 no visible effect; 1, 2, 3 slight injury, plant usually recovered with little or no reduction in top growth; 4, 5, 6 moderate injury, plants usually recovered but with reduced top growth; 7, 8, 9 severe injury, plants usually did not recover; 1O all plants killed.
Test results for various weeds are set out in Table 1:
EXAMPLE rv Bean plants, Phaseolus vulgaris, grown from seeds under greenhouse conditions and in their true leaf stage were used as test plants in order to determine the viricidal activity of 2,3-dichloro-N-isopropylthiocarboxy maleimide.
The maleimide being tested was dissolved in a solvent composition comprised of 4 milliliters sorbitan trioleate (Span 85), l milliliter of a polyoxyalkylene derivative of sorbitan monooleate (Tween 80), and 1995 mi]- liliters of acetone. After dissolving the test compound in the solvent at the desired concentration, the solution was applied to the test plants with a spraying device having a pressurized valve control at 40 pounds pressure for 60 seconds, thereby assuring complete coverage of the plant surface. After the treated plants had air dried, they were inoculated by spraying with extract from tobacco mosaic virus infected leaves and carborundum. The carborundum, which was kept in suspension by constant agitation of the solution, caused the surface tissue of the plant to rupture with gentle rubbing and thus provided sites for the virus to attack the leaves.
Untreated plants and plants inoculated as above were used as controls. Disease severity was determined by actual count of infection loci on inoculated plants. Control effectiveness of the compound is expressed as per cent virus control and is determined by a count of infection loci on treated plants compared with equivalent counts of infection loci on inoculated but otherwise untreated controls. Each reported result is the average of three replicate tests.
An initial evaluation at 1000 ppm gave 95 per cent control. A subsequent retest was undertaken at 1,000, 500, and 250 ppm with 63 per cent, 26 per cent, and 41 per cent control resulting. A retest on tobacco plants, Nicotiana glurinosa, at 500, 250, and 100 ppm gave 26 per cent, per cent, and 0 per cent control.
I claim:
1. A halogenated N-substituted thiocarboxy maleimide represented by the formula:
where X is halogen; X is halogen or H; and R is alkyl, alkenyl, cycloalkyl, cycloalkenyl, haloalkyl, haloalkenyl, phenyl, alkyl phenyl, alkoxyphenyl or halophenyl containing 12 carbon atoms or less, which comprises reacting a halogenated maleimide of the formula:
where X and X are as defined as above with a chlorothioformate of the formula where R is defined as above, in an inert solvent and in the presence of an acid acceptor.

Claims (5)

1. A HALOGENATED N-SUBSTITUTED THIOCARBOXY MALEIMIDE REPRESENTED BY THE FORMULA:
2. The compounds of claim 1 where R is an alkyl or alkenyl group containing from 1 to 6 carbon atoms.
3. The compounds of claim 1 wherein R is methyl, 2-chloroethyl, isopropyl, 2,3-dibromo butyl, or 2-chloro-3-hexenyl.
4. 2,3-dichloro-N-isopropylthiocarboxy maleimide.
5. A method of preparing 2-halo and 2,3-dihalo-N-substituted thiocarboxy maleimides of the formula:
US317571A 1972-12-22 1972-12-22 Halogenated N-substituted thiocarboxy maleimides Expired - Lifetime US3882145A (en)

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Cited By (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3966954A (en) * 1973-09-21 1976-06-29 American Cyanamid Company 3,5-Cycloalkyl pyrazolium salts as fungicides
US4003912A (en) * 1973-06-11 1977-01-18 Monsanto Company Dicarboximido-N-phenylsubstituted carbamates and derivatives
JPS54112857A (en) * 1977-07-25 1979-09-04 Chinoin Gyogyszer Es Vegyeszet Novel maleinimide and succinimide derivative
CN102344398A (en) * 2003-12-18 2012-02-08 因赛特公司 3-cycloalkylaminopyrrolidine derivatives as modulators of chemokine receptors
CN102584845A (en) * 2011-12-30 2012-07-18 云南烟草科学研究院 Furan flavonoid compound in nicotiana tobacum and application thereof

Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3340263A (en) * 1964-02-14 1967-09-05 Ciba Geigy Corp Amino-pyrroles

Patent Citations (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3340263A (en) * 1964-02-14 1967-09-05 Ciba Geigy Corp Amino-pyrroles

Cited By (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4003912A (en) * 1973-06-11 1977-01-18 Monsanto Company Dicarboximido-N-phenylsubstituted carbamates and derivatives
US3966954A (en) * 1973-09-21 1976-06-29 American Cyanamid Company 3,5-Cycloalkyl pyrazolium salts as fungicides
JPS54112857A (en) * 1977-07-25 1979-09-04 Chinoin Gyogyszer Es Vegyeszet Novel maleinimide and succinimide derivative
US4353734A (en) * 1977-07-25 1982-10-12 Chinoin Gyogyszer Es Vegyeszeti Termekek Gyara R.T. Maleimide and succinimide derivatives and herbicidal method of use thereof
CN102344398A (en) * 2003-12-18 2012-02-08 因赛特公司 3-cycloalkylaminopyrrolidine derivatives as modulators of chemokine receptors
CN102344398B (en) * 2003-12-18 2015-02-25 因赛特公司 3-cycloalkylaminopyrrolidine derivatives as modulators of chemokine receptors
CN102584845A (en) * 2011-12-30 2012-07-18 云南烟草科学研究院 Furan flavonoid compound in nicotiana tobacum and application thereof
CN102584845B (en) * 2011-12-30 2014-09-24 云南烟草科学研究院 A kind of furan flavonoid compound in tobacco and application thereof

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